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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Acid → 4,5,6,7-Tetrahydro-2-benzimidazolone

HRID 1683352
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HRID 1683352 반응식
Br[CH:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C:3]1=O.[NH2:9][C:10]([NH2:12])=[O:11].C([O-])(=O)C.[NH4+].C(O)(=O)C>O>[N:9]1[C:10](=[O:11])[N:12]=[C:2]2[CH2:7][CH2:6][CH2:5][CH2:4][C:3]=12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 1176UreaHCID 517165Ammonium AcetateHCID 117897582-Bromocyclohexanone

생성물 1

HCID 232922894,5,6,7-Tetrahydro-2-benzimidazolone

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 2-bromocyclohexanone (6.23 g, 0.035 mol) and urea (2.1 g, 0.035 mol) is refluxed in a solution of ammonium acetate (10 g), acetic acid (15 mL) and water (50 mL) for 4 h. Upon cooling slowly to room temp, white crystals form in the reaction vessel. The solid is collected by suction filtration, washed thoroughly with water and ether, and dried in vacuo to afford 4,5,6,7-tetrahydro-2-benzimidazolone (Compound 7).

후처리

  1. filtrationThe solid is collected by suction filtration
  2. washwashed thoroughly with water and ether
  3. customdried in vacuo

출처 및 근거

ORD 기록
ord-4314b798c9844be48a37a26ffe395954
출처 데이터셋
uspto-grants-1997_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05637725

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